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Efficacy of Caffeine, With and Without Biperiden, in the Detoxification of Cocaine Dependent Patients

Efficacy of Caffeine, With and Without Biperiden, in the Detoxification of Cocaine Dependent Patients

Status
Completed
Phases
Phase 2Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00495092
Enrollment
85
Registered
2007-07-02
Start date
2005-01-31
Completion date
2010-10-31
Last updated
2012-03-01

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cocaine Related Disorders

Keywords

cocaine dependence, cocaine use, cocaine craving

Brief summary

The aim of this study is to assess the efficacy of caffeine compared to placebo in detoxifying cocaine dependent patients. Caffeine potentiation with biperiden will be also studied. 108 with cocaine dependence will be randomized to receive caffeine (300 - 1200 mg t.i.d.) plus biperidene (8 mg b.i.d.) or caffeine (300 - 1200 mg t.i.d.) with placebo or placebo during 6 months. Primary efficacy outcomes will be 1) patient comfort assessed with abstinence symptomatology, craving for cocaine and mental status during detoxifying period, 2) study retention and 3) cocaine use. Brain dopamine system will be assessed thru IBZM-SPECT and the apomorphine test.

Interventions

DRUGCaffeine

Caffeine from 300 mg/d to 1200 mg/d or 15 mg/kg/d

Biperiden 2-4 mg/d p.o.

DRUGPlacebo

Placebo + Placebo

Sponsors

Hospital Universitari Vall d'Hebron Research Institute
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
TRIPLE (Subject, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 60 Years
Healthy volunteers
No

Inclusion criteria

* diagnosis of intranasal cocaine dependence, according to DSM-IV-TR criteria * age between 18 and 60 years * current cocaine use, confirmed by a positive urine drug screen for cocaine the week prior to admission. * demonstrated capacity to grant informed consent and sign the pertinent informed consent form. * place of residence compatible with attendance at the centre. * for women, willingness to use effective contraceptive measures during the study.

Exclusion criteria

* diagnosis of a severe medical disorder that could interfere with the study * presence of an organic pathology for which methylxanthines or biperidene, iodine or apomorphine administration is contraindicated * serum liver transaminase levels 3 times higher than normal values * pregnancy and breast-feeding * neuroleptic medication treatment in the past 6 weeks * current treatment, or anticipation that the patient may need to initiate treatment during the study with drugs that may interact with study medication. * current diagnosis of a major mental disorder. * awareness of a situation that could prevent the patient's participation in the study (e.g. serving a sentence) * current participation in another research project.

Design outcomes

Primary

MeasureTime frame
1) comfort with cocaine detox defined as cocaine abstinence symptoms, cocaine craving, depressive symptoms and anxiety symptoms 2) study retention and 3) cocaine use.12-14 days for primary otcome num 1 and 23 weeks for num 2 and 3.

Countries

Spain

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026